The effect of a new bone material in the treatment of bony defects caused by periodontal disease
Not Applicable
Completed
- Conditions
- Chronic periodontitis.Chronic Periodontits
- Registration Number
- IRCT2015102024622N1
- Lead Sponsor
- Samareh Kafilzadeh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Patients with at least one vertical defect assessed by clinical and radiographic evaluation
Patients with no systemic disease
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Depth of the defect. Timepoint: at the first surgery and 6 months later at a re-entry surgery. Method of measurement: using a periodontal probe.;Width of the defect. Timepoint: at the first surgery and 6 months later at a re-entry surgery. Method of measurement: using a periodontal probe.
- Secondary Outcome Measures
Name Time Method Keratinized tissue. Timepoint: at the first surgery and 6 months later at a re-entry surgery. Method of measurement: using a periodontal probe.;Plaque index. Timepoint: at the first surgery and 6 months later at a re-entry surgery. Method of measurement: using a periodontal probe.;Gingival recession. Timepoint: at the first surgery and 6 months later at a re-entry surgery. Method of measurement: using a periodontal probe.;Bleeding on probing. Timepoint: at the first surgery and 6 months later at a re-entry surgery. Method of measurement: using a periodontal probe.;Clinical attachment level. Timepoint: at the first surgery and 6 months later at a re-entry surgery. Method of measurement: using a periodontal probe.;Pocket depth. Timepoint: at the first surgery and 6 months later at a re-entry surgery. Method of measurement: using a periodontal probe.